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Hydrochloric Acid → 3-{4-[3-(3-Bromophenyl)-1-(4-cyclohex-1-enylphenyl)ureidomethyl]benzoylamino}propionic acid

HRID 49551
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반응식

HRID 49551 반응식
C[O:2][C:3](=[O:39])[CH2:4][CH2:5][NH:6][C:7](=[O:38])[C:8]1[CH:13]=[CH:12][C:11]([CH2:14][N:15]([C:26]2[CH:31]=[CH:30][C:29]([C:32]3[CH2:37][CH2:36][CH2:35][CH2:34][CH:33]=3)=[CH:28][CH:27]=2)[C:16]([NH:18][C:19]2[CH:24]=[CH:23][CH:22]=[C:21]([Br:25])[CH:20]=2)=[O:17])=[CH:10][CH:9]=1.[OH-].[Li+].Cl>C1COCC1.O>[Br:25][C:21]1[CH:20]=[C:19]([NH:18][C:16](=[O:17])[N:15]([CH2:14][C:11]2[CH:10]=[CH:9][C:8]([C:7]([NH:6][CH2:5][CH2:4][C:3]([OH:39])=[O:2])=[O:38])=[CH:13][CH:12]=2)[C:26]2[CH:27]=[CH:28][C:29]([C:32]3[CH2:37][CH2:36][CH2:35][CH2:34][CH:33]=3)=[CH:30][CH:31]=2)[CH:24]=[CH:23][CH:22]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 3939Lithium Hydroxide2회HCID 67483870HCID 67483870, 화합물

생성물 1

HCID 101208673-{4-[3-(3-Bromophenyl)-1-(4-cyclohex-1-enylphenyl)ureidomethyl]benzoylamino}propionic acid수율 61%

시약·촉매·용매 2

HCID 962Water용매2회
HCID 8028
Tetrahydrofuran
용매

실험 절차

3-{4-[3-(3-Bromophenyl)-1-(4-cyclohex-1-enylphenyl)ureidomethyl]benzoylamino}propionic acid methyl ester (0.64 g, 1.08 mmol) was dissolved in THF (10 ml) and lithium hydroxide (0.043 g, 1.08 mmol) in water (1 ml) was added and the resulting mixture was stirred at room temperature for 16 hours. More lithium hydroxide (0.043 g, 1.08 mmol) in water (1 ml) was added and, after 4 hours, 1N hydrochloric acid (2.2 ml) was added. The mixture was concentrated in vacuo and the residue was triturated with water, filtered and dried in vacuo at 40° C. to afford 0.378 g (61%) of 3-{4-[3-(3-bromophenyl)-1-(4-cyclohex-1-enylphenyl)ureidomethyl]benzoylamino}propionic acid.

후처리

  1. concentrationThe mixture was concentrated in vacuo
  2. customthe residue was triturated with water
  3. filtrationfiltered
  4. customdried in vacuo at 40° C.

출처 및 근거

ORD 기록
ord-246957b59fd44eb9a670730f9625d210
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06706744B2

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